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Allwin Embryo Transfer Catheters (ETC), Allwin ETC Stylets and Soft Obturators

K200248 Class II Traditional
Decision Date
2020-07-01
Sponsor / Applicant
Allwin Medical Devices, Inc.

Technical Specification

510(k) Submission ID K200248
Product Code MQF
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6110
Decision Date 2020-07-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Allwin Embryo Transfer Catheters (ETC), Allwin ETC Stylets and Soft Obturators received FDA 510(k) clearance under submission number K200248, sponsored by Allwin Medical Devices, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2020-07-01.

Classification & Regulation

This clearance is catalogued under FDA product code MQF and 21 CFR 884.6110, within the Obstetrics/Gynecology review panel as a Class II device.